Orange Book product
FOAMICON 80MG;20MG
Orange Book ANDA 072687 · NOVARTIS CONSUMER HEALTH INC · Discontinued
Key facts
| Proprietary name | FOAMICON |
|---|---|
| Active ingredients | ALUMINUM HYDROXIDE, MAGNESIUM TRISILICATE |
| Strength | 80MG;20MG |
| Dosage form | TABLET, CHEWABLE |
| Route | ORAL |
| Application | ANDA072687 |
| Applicant holder | NOVARTIS CONSUMER HEALTH INC |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Jun 28, 1989 |
At a glance
- None Marketed products with the same ingredient, strength and form
- 1–9 Products in this application
- No Reference listed drug
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Orange Book products
The FDA Orange Book lists approved drug products with their therapeutic equivalence (TE) codes, reference listed drugs and marketing status. Products approved before 1982 show an approval date of Jan 1, 1982.